NO20064676L - Pharmaceutical salts of 3-O- (3'3'-dimethylsuccinyl) betulinic acid - Google Patents
Pharmaceutical salts of 3-O- (3'3'-dimethylsuccinyl) betulinic acidInfo
- Publication number
- NO20064676L NO20064676L NO20064676A NO20064676A NO20064676L NO 20064676 L NO20064676 L NO 20064676L NO 20064676 A NO20064676 A NO 20064676A NO 20064676 A NO20064676 A NO 20064676A NO 20064676 L NO20064676 L NO 20064676L
- Authority
- NO
- Norway
- Prior art keywords
- dimethylsuccinyl
- betulinic acid
- dsb
- pharmaceutical salts
- salts
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 4
- QGJZLNKBHJESQX-UHFFFAOYSA-N 3-Epi-Betulin-Saeure Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C(=C)C)C5C4CCC3C21C QGJZLNKBHJESQX-UHFFFAOYSA-N 0.000 title 1
- CLOUCVRNYSHRCF-UHFFFAOYSA-N 3beta-Hydroxy-20(29)-Lupen-3,27-oic acid Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C(O)=O)CCC5(C)CCC(C(=C)C)C5C4CCC3C21C CLOUCVRNYSHRCF-UHFFFAOYSA-N 0.000 title 1
- DIZWSDNSTNAYHK-XGWVBXMLSA-N Betulinic acid Natural products CC(=C)[C@@H]1C[C@H]([C@H]2CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12)C(=O)O DIZWSDNSTNAYHK-XGWVBXMLSA-N 0.000 title 1
- QGJZLNKBHJESQX-FZFNOLFKSA-N betulinic acid Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C(=C)C)[C@@H]5[C@H]4CC[C@@H]3[C@]21C QGJZLNKBHJESQX-FZFNOLFKSA-N 0.000 title 1
- PZXJOHSZQAEJFE-UHFFFAOYSA-N dihydrobetulinic acid Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C(C)C)C5C4CCC3C21C PZXJOHSZQAEJFE-UHFFFAOYSA-N 0.000 title 1
- MQYXUWHLBZFQQO-UHFFFAOYSA-N nepehinol Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C)CCC(C(=C)C)C5C4CCC3C21C MQYXUWHLBZFQQO-UHFFFAOYSA-N 0.000 title 1
- YJEJKUQEXFSVCJ-WRFMNRASSA-N bevirimat Chemical compound C1C[C@H](OC(=O)CC(C)(C)C(O)=O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C(=C)C)[C@@H]5[C@H]4CC[C@@H]3[C@]21C YJEJKUQEXFSVCJ-WRFMNRASSA-N 0.000 abstract 2
- 238000011156 evaluation Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 159000000011 group IA salts Chemical group 0.000 abstract 1
- 238000001727 in vivo Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
- C07J63/008—Expansion of ring D by one atom, e.g. D homo steroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
- C08B37/0012—Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/16—Cyclodextrin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Polymers & Plastics (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Virology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Materials Engineering (AREA)
- Biochemistry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Det beskrives salter av 3-O-(3',3'-dimetylsuccinyl) betulinsyre (DSB). Spesielt beskrives fremstilling, farmasøytisk evaluering og in vivo biotilgjengelighetsevaluering av N-metyl-D-glucamin og alkaliesaltformer av DSB. Videre beskrives farmasøytiske preparater inkludert disse saltformer for anvendelse i metoder for behandling av HIV og relaterte sykdommer. Det tilveiebringes også metoder for å fremstille saltene av DSB og også de farmasøytiske preparater.Salts of 3-O- (3 ', 3'-dimethylsuccinyl) betulinic acid (DSB) are described. Specifically, the preparation, pharmaceutical evaluation and in vivo bioavailability evaluation of N-methyl-D-glucamine and alkaline salt forms of DSB are described. Further, pharmaceutical compositions including these salt forms are disclosed for use in methods of treating HIV and related diseases. Methods are also provided for preparing the salts of DSB and also the pharmaceutical preparations.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55355404P | 2004-03-17 | 2004-03-17 | |
US58467404P | 2004-07-02 | 2004-07-02 | |
PCT/US2005/008935 WO2005090380A1 (en) | 2004-03-17 | 2005-03-17 | Pharmaceuticals salts of 3-o-(3',3'-dimethylsuccinyl) betulinic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20064676L true NO20064676L (en) | 2006-12-01 |
Family
ID=34993638
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20064676A NO20064676L (en) | 2004-03-17 | 2006-10-16 | Pharmaceutical salts of 3-O- (3'3'-dimethylsuccinyl) betulinic acid |
Country Status (11)
Country | Link |
---|---|
US (2) | US20050239748A1 (en) |
EP (1) | EP1730163A4 (en) |
JP (1) | JP2007529544A (en) |
AU (1) | AU2005224260A1 (en) |
BR (1) | BRPI0508854A (en) |
CA (1) | CA2560266A1 (en) |
IL (1) | IL178128A0 (en) |
MX (1) | MXPA06010592A (en) |
NO (1) | NO20064676L (en) |
RU (1) | RU2387665C2 (en) |
WO (1) | WO2005090380A1 (en) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
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ES2383534T3 (en) * | 2005-04-12 | 2012-06-22 | Myrexis, Inc. | 3-O- (3 ', 3'-dimethylsuccinyl) betulinic acid di-N-methyl-D-glucamine polymorphs |
BRPI0619936A2 (en) * | 2005-12-16 | 2011-10-25 | Panacos Pharmaceuticals Inc | preparation of pharmaceutical salts of 3-o- (3 ', 3'-dimethylsuccinyl) betulinic acid |
US20080039428A1 (en) * | 2006-06-29 | 2008-02-14 | Panacos Pharmaceuticals, Inc. | Antiretroviral combination therapy |
CZ300722B6 (en) * | 2006-09-27 | 2009-07-22 | Univerzita Karlova v Praze, Prírodovedecká fakulta | Process for preparing inclusion complex of pentacyclic and tetracyclic terpenoids, process for preparing pharmaceutical composition containing this inclusion complex, inclusion complex of pentacyclic or tetracyclic terpenoid and pharmaceutical compos |
TW200837074A (en) | 2006-11-03 | 2008-09-16 | Panacos Pharmaceuticals Inc | Extended triterpene derivatives |
WO2008091532A1 (en) * | 2007-01-19 | 2008-07-31 | Panacos Pharmaceuticals, Inc. | Salts of 3-o-(3',3'-dimethylsuccinyl)betulinic acid and solid state forms thereof |
WO2012106190A1 (en) | 2011-01-31 | 2012-08-09 | Bristol-Myers Squibb Company | C-17 and c-3 modified triterpenoids with hiv maturation inhibitory activity |
WO2009042166A1 (en) * | 2007-09-25 | 2009-04-02 | Panacos Pharmaceuticals, Inc. | Liquid bevirimat dosage forms for oral administration |
JP2009120516A (en) * | 2007-11-13 | 2009-06-04 | Tokyo Medical Univ | Antiviral agent |
US8802727B2 (en) * | 2009-07-14 | 2014-08-12 | Hetero Research Foundation, Hetero Drugs Limited | Pharmaceutically acceptable salts of betulinic acid derivatives |
US9067966B2 (en) | 2009-07-14 | 2015-06-30 | Hetero Research Foundation, Hetero Drugs Ltd. | Lupeol-type triterpene derivatives as antivirals |
EA026140B1 (en) | 2010-06-04 | 2017-03-31 | Бристол-Майерс Сквибб Компани | C-28 amides of modified c-3 betulinic acid derivatives as hiv maturation inhibitors |
JP5752789B2 (en) * | 2010-06-04 | 2015-07-22 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Modified C-3 betulinic acid derivatives as HIV maturation inhibitors |
US20140221328A1 (en) * | 2011-01-10 | 2014-08-07 | Bandi Parthasaradhi Reddy | Pharmaceutically acceptable salts of novel betulinic acid derivatives |
WO2012106188A1 (en) | 2011-01-31 | 2012-08-09 | Bristol-Myers Squibb Company | C-28 amines of c-3 modified betulinic acid derivatives as hiv maturation inhibitors |
RU2489147C2 (en) * | 2011-08-31 | 2013-08-10 | Людмила Петровна Лазурина | Local pharmaceutical antibacterial composition of active biometallic complexes |
ES2611727T3 (en) | 2011-09-21 | 2017-05-10 | VIIV Healthcare UK (No.5) Limited | Novel betulinic acid derivatives with antiviral activity |
US8906889B2 (en) | 2012-02-15 | 2014-12-09 | Bristol-Myers Squibb Company | C-3 cycloalkenyl triterpenoids with HIV maturation inhibitory activity |
US8889854B2 (en) | 2012-05-07 | 2014-11-18 | Bristol-Myers Squibb Company | C-17 bicyclic amines of triterpenoids with HIV maturation inhibitory activity |
WO2014105926A1 (en) | 2012-12-31 | 2014-07-03 | Hetero Research Foundation | Novel betulinic acid proline derivatives as hiv inhibitors |
CN105121454A (en) | 2013-02-06 | 2015-12-02 | 百时美施贵宝公司 | C-19 modified triterpenoids with HIV maturation inhibitory activity |
EP2958930A1 (en) | 2013-02-25 | 2015-12-30 | Bristol-Myers Squibb Company | C-3 alkyl and alkenyl modified betulinic acid derivatives useful in the treatment of hiv |
KR102411082B1 (en) | 2014-04-11 | 2022-06-17 | 비브 헬스케어 유케이 (넘버4) 리미티드 | Triterpenoids with hiv maturation inhibitory activity, substituted in position 3 by a non-aromatic ring carrying a haloalkyl substituent |
US9920090B2 (en) | 2014-06-19 | 2018-03-20 | VIIV Healthcare UK (No.5) Limited | Betulinic acid derivatives with HIV maturation inhibitory activity |
US20170129916A1 (en) | 2014-06-26 | 2017-05-11 | Hetero Research Foundation | Novel betulinic proline imidazole derivatives as hiv inhibitors |
WO2016077561A1 (en) | 2014-11-14 | 2016-05-19 | Bristol-Myers Squibb Company | Oxolupene derivatives |
BR112017009852A2 (en) | 2014-11-14 | 2018-01-16 | Viiv Healthcare Uk No 5 Ltd | compound, composition, and uses of a compound |
MA40886B1 (en) | 2015-02-09 | 2020-03-31 | Hetero Research Foundation | Novel c-3 triterpenone with c-28 reverse amide derivatives as hiv inhibitors |
WO2016147099A2 (en) | 2015-03-16 | 2016-09-22 | Hetero Research Foundation | C-3 novel triterpenone with c-28 amide derivatives as hiv inhibitors |
AR107512A1 (en) | 2016-02-04 | 2018-05-09 | VIIV HEALTHCARE UK Nº 5 LTD | TRITERPENOIDS MODIFIED IN C-3 AND C-17 AS HIV-1 INHIBITORS |
CN107625967B (en) | 2016-07-15 | 2021-07-06 | 中国人民解放军军事医学科学院毒物药物研究所 | A kind of pharmaceutical composition for Tecoviride injection and preparation method thereof |
CN107638571B (en) | 2016-07-15 | 2021-07-06 | 中国人民解放军军事医学科学院毒物药物研究所 | A kind of oral pharmaceutical composition of Tecoviride and preparation method thereof |
CA3075023A1 (en) | 2017-09-14 | 2019-03-21 | Phoenix Biotechnology, Inc. | Method and improved neuroprotective composition for treating neurological conditions |
IL285232B (en) | 2017-09-14 | 2022-07-01 | Phoenix Biotechnology Inc | Preparations containing oleandrin for the treatment of viral infection |
EP3796900A4 (en) | 2018-06-29 | 2022-03-30 | DFH Therapeutics | TRITERPEN AMINE DERIVATIVES |
SG11202105728YA (en) | 2020-03-31 | 2021-11-29 | Phoenix Biotechnology Inc | Method and compositions for treating coronavirus infection |
EP4295854A3 (en) | 2020-03-31 | 2024-04-03 | Phoenix Biotechnology, Inc. | Method and compositions for treating coronavirus infection |
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US3839344A (en) * | 1973-03-28 | 1974-10-01 | Schering Corp | N-methyl d-glucamine salt of 2(2'-methyl-3'-trifluoromethylanilino)nicotinic acid |
US4205073A (en) * | 1975-04-30 | 1980-05-27 | Schering Corporation | Anti-diarrheal anilino nicotinic acids and method of using same |
US4377583A (en) * | 1981-08-21 | 1983-03-22 | Mead Johnson & Company | N-Methyl-D-glucamine salt of with 3,4-dihydro-5-methyl-6-(2-methylpropyl)-4-oxothieno[2,3-d]pyrimidine-2-carboxylic acid |
JPS60163897A (en) * | 1984-02-06 | 1985-08-26 | Tokyo Tanabe Co Ltd | Ursodeoxycholic acid meglumine salt and its injection |
US4727064A (en) * | 1984-04-25 | 1988-02-23 | The United States Of America As Represented By The Department Of Health And Human Services | Pharmaceutical preparations containing cyclodextrin derivatives |
EP0538011B1 (en) * | 1991-10-16 | 1997-07-30 | Schering Corporation | Lipophilic oligosaccharide antibiotic salt compositions |
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US5679828A (en) * | 1995-06-05 | 1997-10-21 | Biotech Research Labs, Inc. | Betulinic acid and dihydrobetulinic acid derivatives and uses therefor |
GB9613455D0 (en) * | 1996-06-27 | 1996-08-28 | Aston Molecules Ltd | Analogues or derivatives of quercetin |
US5776912A (en) * | 1996-12-20 | 1998-07-07 | Schering Corporation | Lipophilic oligosaccharide antibiotic compositions |
US6043245A (en) * | 1997-09-25 | 2000-03-28 | Schering Corporation | Tetrahydrofuran antifungal phosphate |
US6670345B1 (en) * | 1997-09-30 | 2003-12-30 | Dabur Research Foundation | Betulinic acid derivatives for inhabiting cancer growth and process for the manufacture of betulinic acid |
ATE348839T1 (en) * | 1998-03-02 | 2007-01-15 | Univ North Carolina | ACYLATED BETULIN AND DIHYDROBETULIN DERIVATIVES, THEIR PREPARATION AND USE |
WO1999067284A2 (en) * | 1998-06-20 | 1999-12-29 | Washington University | Membrane-permeant peptide complexes for medical imaging, diagnostics, and pharmaceutical therapy |
US6147077A (en) * | 1999-04-29 | 2000-11-14 | Sepracor Inc. | 2R,4S-hydroxyitraconazole isomers |
US6579828B1 (en) * | 1999-10-15 | 2003-06-17 | Nippon Paper Industries Co. Ltd | Multi chromatic thermally sensitive recording medium |
US7276510B2 (en) * | 2000-05-08 | 2007-10-02 | Janssen Pharmaceutica, Inc. | HIV replication inhibitors |
US7365221B2 (en) * | 2002-09-26 | 2008-04-29 | Panacos Pharmaceuticals, Inc. | Monoacylated betulin and dihydrobetulin derivatives, preparation thereof and use thereof |
JP2006520756A (en) * | 2003-01-29 | 2006-09-14 | パナコス ファーマシューティカルズ インコーポレーティッド | Inhibition of HIV-1 replication by disruption of viral capsid spacer peptide 1 protein processing |
US20050148561A1 (en) * | 2003-09-26 | 2005-07-07 | Panacos Pharmaceuticals, Inc. | Novel triterpene derivatives, preparation thereof and use thereof |
RU2243233C1 (en) * | 2003-12-24 | 2004-12-27 | Московская государственная академия тонкой химической технологии им. М.В. Ломоносова | Derivatives of betulin as complement inhibitors |
-
2005
- 2005-03-17 BR BRPI0508854-2A patent/BRPI0508854A/en not_active IP Right Cessation
- 2005-03-17 MX MXPA06010592A patent/MXPA06010592A/en not_active Application Discontinuation
- 2005-03-17 WO PCT/US2005/008935 patent/WO2005090380A1/en active Application Filing
- 2005-03-17 RU RU2006136409/04A patent/RU2387665C2/en not_active IP Right Cessation
- 2005-03-17 AU AU2005224260A patent/AU2005224260A1/en not_active Abandoned
- 2005-03-17 EP EP05728826A patent/EP1730163A4/en not_active Withdrawn
- 2005-03-17 JP JP2007504115A patent/JP2007529544A/en active Pending
- 2005-03-17 CA CA002560266A patent/CA2560266A1/en not_active Abandoned
- 2005-03-17 US US11/081,802 patent/US20050239748A1/en not_active Abandoned
-
2006
- 2006-09-17 IL IL178128A patent/IL178128A0/en unknown
- 2006-10-16 NO NO20064676A patent/NO20064676L/en not_active Application Discontinuation
-
2012
- 2012-04-30 US US13/460,463 patent/US20120214775A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
AU2005224260A1 (en) | 2005-09-29 |
US20120214775A1 (en) | 2012-08-23 |
BRPI0508854A (en) | 2007-08-28 |
EP1730163A1 (en) | 2006-12-13 |
RU2387665C2 (en) | 2010-04-27 |
WO2005090380A1 (en) | 2005-09-29 |
EP1730163A4 (en) | 2009-12-30 |
CA2560266A1 (en) | 2005-09-29 |
JP2007529544A (en) | 2007-10-25 |
RU2006136409A (en) | 2008-04-27 |
US20050239748A1 (en) | 2005-10-27 |
IL178128A0 (en) | 2006-12-31 |
MXPA06010592A (en) | 2007-06-12 |
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